chlordiazepoxide hydrochloride and clidinium bromide

Product NDC
23155-808
11-digit product format
231550808
Labeler code
23155
Product ID
23155-808_d8a7aa0f-4337-7366-e053-2995a90acce3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
chlordiazepoxide hydrochloride and clidinium bromide
Dosage form
CAPSULE
Route
ORAL
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Application
ANDA210579
Marketing category
ANDA
Marketing start
2022-01-01
Marketing end
0000-00-00
Substance
CHLORDIAZEPOXIDE; CLIDINIUM BROMIDE
Active strength
5 mg/1; mg/1
Pharmacologic classes
Anticholinergic [EPC], Benzodiazepine [EPC], Benzodiazepines [CS], Cholinergic Antagonists [MoA], Decreased Parasympathetic Acetylcholine Activity [PE], Digestive/GI System Activity Alteration [PE], GI Motility Alteration [PE]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23155-808-01EA - Each23155-8088636a986-3eaa-438a-a25b-a7cb256197f712022-03-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23155-808-0123155080801100 CAPSULE in 1 BOTTLE, PLASTIC (23155-808-01) 100 capsule2022-01-010000-00-00NoNoCurrent